651-93-4

Basic information

• Product Name: Tetrakis(trifluoromethyl)thiophene
• Synonyms: Tetrakis(trifluoromethyl)thiophene
• CAS NO: 651-93-4
• Molecular Formula: C₈F₁₂S
• Molecular Weight: 0
• Mol File: 651-93-4.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Tetrakis(trifluoromethyl)thiophene(CAS DataBase Reference)
• NIST Chemistry Reference: Tetrakis(trifluoromethyl)thiophene(651-93-4)
• EPA Substance Registry System: Tetrakis(trifluoromethyl)thiophene(651-93-4)

Safety Data

• Hazardous Substances Data: 651-93-4(Hazardous Substances Data)

Upstream product

• 19259-11-1 2,3,4,5-tetraiodo-thiophene 
• 77152-08-0 trifluoromethylcopper(I) 
• 130340-18-0 perfluoro-trans,trans-3,4-dimethylhexa-2,4-diene 
• 661-54-1 3,3,3-trifluoroprop-1-yne 
• 692-50-2 hexafluoro-2-butyne 
• 1768-32-7 sulfur bis(trifluoromethyl)amide chloride 
• 74-86-2 acetylene 
• 24692-18-0 perfluoro-3,4-dimethylhexa-2,4-diene 
• 25543-35-5 1,1,1,2,2,5,5,6,6,6-decafluoro-3,4-bis(trifluoromethyl)-3-heptene 
• 654-60-4 2,3,5,6-tetrakis(trifluoromethyl)-p-dithiine 
• 360-91-8 3,4-bis-trifluoromethyl-[1,2]dithiete 
• 7704-34-9 sulfur 
• 39091-73-1 1,2,3,4-tetrakis(trifluoromethyl)-5-thiabicyclo{2.1.0}pent-2-ene 

Downstream Products

• 320-23-0 1,2,4,5-tetrakis(trifluoromethyl)benzene 
• 39091-73-1 1,2,3,4-tetrakis(trifluoromethyl)-5-thiabicyclo{2.1.0}pent-2-ene 
• 87721-43-5 1,2,4,6-Tetrakis-trifluoromethyl-3,5,7-trithia-tricyclo[4.1.0.0^2,4]heptane 
• 692-50-2 hexafluoro-2-butyne 

Relevant articles and documents

A Synthesis of Novel Perfluorodienes

Oligomers of perfluoroalkenes are converted to dienes in good yields, using sodium amalgam; these dienes are highly susceptible to nucleophilic attack and can be excellent sources of heterocycles.

CYCLIC COMPOUNDS FROM PERFLUORO-3,4-DIMETHYLHEXA-2,4-DIENE

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Fluorinated di-enes

Fluorinated di-enes may be obtained by the defluorination of some oligomers of F-alkenes and -cycloalkenes using tetrakis(dimethylamino)ethene.These di-enes are very susceptible to nucleophilic attack.Nucleophilic epoxidation of (4) gives a new diepoxide which undergoes a novel ring-opening reaction.Di-ene (4) forms cyclopentadienylide derivatives with di-functional carbon nucleophiles and a cyclopentadienylide salt (17) is obtained in a remarkable 'one-pot' reaction from hexachlorobutadiene. (4) (17) - Keywords: Fluorinated di-enes; Tetrakis(dimethylamino)ethene; Defluorination